P5374Genetic deletion of IL-22 increased cardiac rupture after myocardial infarction in mice
Abstract Background Interleukin-22 (IL-22) is a member of the IL-10 cytokine family, which mainly targets epithelial cells and does not target immune cells. Recently, it has been reported that IL-22 play roles in tissue repair in the skin and the liver; however, role of IL-22 in the process of tissu...
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| Veröffentlicht in: | European heart journal 2019-10, Vol.40 (Supplement_1) |
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| creator | Yamamoto, M Yasukawa, H Takahashi, J Nohara, S Sasak, T Shimozono, K Shibata, T Yanai, T Okabe, K Mawatari, K Fukumoto, Y |
| description | Abstract
Background
Interleukin-22 (IL-22) is a member of the IL-10 cytokine family, which mainly targets epithelial cells and does not target immune cells. Recently, it has been reported that IL-22 play roles in tissue repair in the skin and the liver; however, role of IL-22 in the process of tissue repair after myocardial infarction (MI) is unknown. Here, we investigated the role of IL-22 in tissue repair process after MI.
Methods and results
First, we examined the expression of IL-22 and its receptor IL-22RA1 in the wild type (WT) mice by real-time PCR. The expression of IL-22 and IL-22RA1 in the hearts were significantly increased 3 days after MI (p |
| doi_str_mv | 10.1093/eurheartj/ehz746.0337 |
| format | Article |
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Background
Interleukin-22 (IL-22) is a member of the IL-10 cytokine family, which mainly targets epithelial cells and does not target immune cells. Recently, it has been reported that IL-22 play roles in tissue repair in the skin and the liver; however, role of IL-22 in the process of tissue repair after myocardial infarction (MI) is unknown. Here, we investigated the role of IL-22 in tissue repair process after MI.
Methods and results
First, we examined the expression of IL-22 and its receptor IL-22RA1 in the wild type (WT) mice by real-time PCR. The expression of IL-22 and IL-22RA1 in the hearts were significantly increased 3 days after MI (p<0.05). To clarify the role of IL-22 in the heart after MI, we produced MI model in the WT mice and IL-22 knockout (KO) mice. We found that the IL-22 KO mice had significantly higher mortality than the WT mice after MI (p<0.05). Approximately 80% of the IL-22 KO mice died with cardiac rupture after MI. The infarct size which was estimated by evans blue dye and triphenyltetrazolium chloride staining at 3 days after MI was comparable between the IL-22 KO mice and the WT mice. Next, we performed real time PCR and PCR array analysis for tissue fibrosis and repair genes. We found that alpha-smooth muscle actin (aSMA), NF-kB, TNF-a and MMP13 (also known as collagenase-3) were significantly increased in the infarct area of IL-22 KO mice compared to WT mice. Immunostaining showed that the myofibroblast marker aSMA positive cells in the border area after MI were markedly higher in the IL-22 KO mice compared with the WT mice (p<0.05). Approximately 70% of cardiac rupture after MI in the IL-22 KO mice were occurred in the infarct area adjacent to the border area. Furthermore, we found aSMA positive cells and MMP13 positive cells around the ruptured site of the heart.
Conclusion
Thus, IL-22 KO mice exhibit high mortality and increased cardiac rupture after MI. And expression of aSMA and MMP13 were highly expressed in the ruptured site after MI in the IL-22 KO mice. These results suggest that IL-22 may play an important role in the tissue repair process after MI.</description><identifier>ISSN: 0195-668X</identifier><identifier>EISSN: 1522-9645</identifier><identifier>DOI: 10.1093/eurheartj/ehz746.0337</identifier><language>eng</language><publisher>Oxford University Press</publisher><ispartof>European heart journal, 2019-10, Vol.40 (Supplement_1)</ispartof><rights>Published on behalf of the European Society of Cardiology. All rights reserved. © The Author(s) 2019. For permissions, please email: journals.permissions@oup.com. 2019</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,777,781,1579,27905,27906</link.rule.ids></links><search><creatorcontrib>Yamamoto, M</creatorcontrib><creatorcontrib>Yasukawa, H</creatorcontrib><creatorcontrib>Takahashi, J</creatorcontrib><creatorcontrib>Nohara, S</creatorcontrib><creatorcontrib>Sasak, T</creatorcontrib><creatorcontrib>Shimozono, K</creatorcontrib><creatorcontrib>Shibata, T</creatorcontrib><creatorcontrib>Yanai, T</creatorcontrib><creatorcontrib>Okabe, K</creatorcontrib><creatorcontrib>Mawatari, K</creatorcontrib><creatorcontrib>Fukumoto, Y</creatorcontrib><title>P5374Genetic deletion of IL-22 increased cardiac rupture after myocardial infarction in mice</title><title>European heart journal</title><description>Abstract
Background
Interleukin-22 (IL-22) is a member of the IL-10 cytokine family, which mainly targets epithelial cells and does not target immune cells. Recently, it has been reported that IL-22 play roles in tissue repair in the skin and the liver; however, role of IL-22 in the process of tissue repair after myocardial infarction (MI) is unknown. Here, we investigated the role of IL-22 in tissue repair process after MI.
Methods and results
First, we examined the expression of IL-22 and its receptor IL-22RA1 in the wild type (WT) mice by real-time PCR. The expression of IL-22 and IL-22RA1 in the hearts were significantly increased 3 days after MI (p<0.05). To clarify the role of IL-22 in the heart after MI, we produced MI model in the WT mice and IL-22 knockout (KO) mice. We found that the IL-22 KO mice had significantly higher mortality than the WT mice after MI (p<0.05). Approximately 80% of the IL-22 KO mice died with cardiac rupture after MI. The infarct size which was estimated by evans blue dye and triphenyltetrazolium chloride staining at 3 days after MI was comparable between the IL-22 KO mice and the WT mice. Next, we performed real time PCR and PCR array analysis for tissue fibrosis and repair genes. We found that alpha-smooth muscle actin (aSMA), NF-kB, TNF-a and MMP13 (also known as collagenase-3) were significantly increased in the infarct area of IL-22 KO mice compared to WT mice. Immunostaining showed that the myofibroblast marker aSMA positive cells in the border area after MI were markedly higher in the IL-22 KO mice compared with the WT mice (p<0.05). Approximately 70% of cardiac rupture after MI in the IL-22 KO mice were occurred in the infarct area adjacent to the border area. Furthermore, we found aSMA positive cells and MMP13 positive cells around the ruptured site of the heart.
Conclusion
Thus, IL-22 KO mice exhibit high mortality and increased cardiac rupture after MI. And expression of aSMA and MMP13 were highly expressed in the ruptured site after MI in the IL-22 KO mice. These results suggest that IL-22 may play an important role in the tissue repair process after MI.</description><issn>0195-668X</issn><issn>1522-9645</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><recordid>eNqNkM1Kw0AUhQdRMFYfQZgXSDuTzO9SitZCQBdduBDCzcwdmtImYZIs6tObGnHt6izu-S6Hj5BHzpac2XyFY9wjxOGwwv2XFmrJ8lxfkYTLLEutEvKaJIxbmSplPm7JXd8fGGNGcZWQz3eZa7HBBofaUY_HKduGtoFuizTLaN24iNCjpw6ir8HROHbDGJFCGDDS07mdD8epGiC6H7xu6Kl2eE9uAhx7fPjNBdm9PO_Wr2nxttmun4rUGa1TLawRILgBqDSAzgwYL5iSNjA37bYuk1ZghT5wpQ14q5xh3HOjnDdQ5Qsi57cutn0fMZRdrE8QzyVn5cVQ-WeonA2VF0MTx2auHbt_It-qxm57</recordid><startdate>20191001</startdate><enddate>20191001</enddate><creator>Yamamoto, M</creator><creator>Yasukawa, H</creator><creator>Takahashi, J</creator><creator>Nohara, S</creator><creator>Sasak, T</creator><creator>Shimozono, K</creator><creator>Shibata, T</creator><creator>Yanai, T</creator><creator>Okabe, K</creator><creator>Mawatari, K</creator><creator>Fukumoto, Y</creator><general>Oxford University Press</general><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>20191001</creationdate><title>P5374Genetic deletion of IL-22 increased cardiac rupture after myocardial infarction in mice</title><author>Yamamoto, M ; Yasukawa, H ; Takahashi, J ; Nohara, S ; Sasak, T ; Shimozono, K ; Shibata, T ; Yanai, T ; Okabe, K ; Mawatari, K ; Fukumoto, Y</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c877-74984a418aab7aa728a8d40659f0c0199c2594ebedf1678ad96c801d186cd8ab3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Yamamoto, M</creatorcontrib><creatorcontrib>Yasukawa, H</creatorcontrib><creatorcontrib>Takahashi, J</creatorcontrib><creatorcontrib>Nohara, S</creatorcontrib><creatorcontrib>Sasak, T</creatorcontrib><creatorcontrib>Shimozono, K</creatorcontrib><creatorcontrib>Shibata, T</creatorcontrib><creatorcontrib>Yanai, T</creatorcontrib><creatorcontrib>Okabe, K</creatorcontrib><creatorcontrib>Mawatari, K</creatorcontrib><creatorcontrib>Fukumoto, Y</creatorcontrib><collection>CrossRef</collection><jtitle>European heart journal</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Yamamoto, M</au><au>Yasukawa, H</au><au>Takahashi, J</au><au>Nohara, S</au><au>Sasak, T</au><au>Shimozono, K</au><au>Shibata, T</au><au>Yanai, T</au><au>Okabe, K</au><au>Mawatari, K</au><au>Fukumoto, Y</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>P5374Genetic deletion of IL-22 increased cardiac rupture after myocardial infarction in mice</atitle><jtitle>European heart journal</jtitle><date>2019-10-01</date><risdate>2019</risdate><volume>40</volume><issue>Supplement_1</issue><issn>0195-668X</issn><eissn>1522-9645</eissn><abstract>Abstract
Background
Interleukin-22 (IL-22) is a member of the IL-10 cytokine family, which mainly targets epithelial cells and does not target immune cells. Recently, it has been reported that IL-22 play roles in tissue repair in the skin and the liver; however, role of IL-22 in the process of tissue repair after myocardial infarction (MI) is unknown. Here, we investigated the role of IL-22 in tissue repair process after MI.
Methods and results
First, we examined the expression of IL-22 and its receptor IL-22RA1 in the wild type (WT) mice by real-time PCR. The expression of IL-22 and IL-22RA1 in the hearts were significantly increased 3 days after MI (p<0.05). To clarify the role of IL-22 in the heart after MI, we produced MI model in the WT mice and IL-22 knockout (KO) mice. We found that the IL-22 KO mice had significantly higher mortality than the WT mice after MI (p<0.05). Approximately 80% of the IL-22 KO mice died with cardiac rupture after MI. The infarct size which was estimated by evans blue dye and triphenyltetrazolium chloride staining at 3 days after MI was comparable between the IL-22 KO mice and the WT mice. Next, we performed real time PCR and PCR array analysis for tissue fibrosis and repair genes. We found that alpha-smooth muscle actin (aSMA), NF-kB, TNF-a and MMP13 (also known as collagenase-3) were significantly increased in the infarct area of IL-22 KO mice compared to WT mice. Immunostaining showed that the myofibroblast marker aSMA positive cells in the border area after MI were markedly higher in the IL-22 KO mice compared with the WT mice (p<0.05). Approximately 70% of cardiac rupture after MI in the IL-22 KO mice were occurred in the infarct area adjacent to the border area. Furthermore, we found aSMA positive cells and MMP13 positive cells around the ruptured site of the heart.
Conclusion
Thus, IL-22 KO mice exhibit high mortality and increased cardiac rupture after MI. And expression of aSMA and MMP13 were highly expressed in the ruptured site after MI in the IL-22 KO mice. These results suggest that IL-22 may play an important role in the tissue repair process after MI.</abstract><pub>Oxford University Press</pub><doi>10.1093/eurheartj/ehz746.0337</doi></addata></record> |
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| title | P5374Genetic deletion of IL-22 increased cardiac rupture after myocardial infarction in mice |
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